P. Grigorescu-Sido

发表

Osteoarthropathy in mucopolysaccharidosis type II

C. Lazea, Ioana Nașcu, P. Grigorescu-Sido, 2013, Clujul medical.

Cardiac Manifestations in a Group of Romanian Patients with Gaucher Disease Type 1 (a Monocentric Study)

Ș. Vesa, C. Lazea, A. Zimmermann, 2021, Diagnostics.

Alterations in Lipid and Carbohydrate Metabolism in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

K. Lackner, H. Rossmann, Matthias M. Weber, 2010, Hormone Research in Paediatrics.

Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)

C. Lazea, R. Popp, P. Grigorescu-Sido, 2017, Therapeutics and clinical risk management.

Association between Cardiac Malformations and Karyotype in Turner Syndrome - a Single Centre Study

C. Lazea, V. Creț, P. Grigorescu-Sido, 2021 .

Biochemical markers of bone turnover as tools in the evaluation of skeletal involvement in patients with type 1 Gaucher disease.

C. Caillaud, A. Crăciun, P. Grigorescu-Sido, 2002, Blood cells, molecules & diseases.

Cholelithiasis in Patients with Gaucher Disease type 1: Risk Factors and the Role of ABCG5/ABCG8 Gene Variants.

P. Galle, D. Leucuta, A. Zimmermann, 2016, Journal of gastrointestinal and liver diseases : JGLD.

INTERLEUKIN 1β, TUMOUR NECROSIS FACTOR-α AND INTERLEUKIN 1 RECEPTOR ANTAGONIST IN NEWLY DIAGNOSED INSULIN-DEPENDENT DIABETES MELLITUS: COMPARISON TO LONG-STANDING DIABETES AND HEALTHY INDIVIDUALS

M. Netea, J. Meer, L. Popa, 1997 .

INSULIN-DEPENDEN T DIABETES MELLITUS: COMPARISON TO LONG-STANDING DIABETES AND HEALTHY INDIVIDUALS

W. Blok, W. Jos, P. Grigorescu-Sido, 1997 .

Evaluation of viral replication in children with chronic hepatitis B with and without interferon treatment.

D. Neculoiu, P. Grigorescu-Sido, C. Lazar, 2005, Romanian journal of gastroenterology.

Laboratory diagnosis and follow-up of Romanian Gaucher disease patients

C. Caillaud, A. Crăciun, T. Drugan, 2017 .

Modelling long-term evolution of chitotriosidase in non-neuronopathic Gaucher disease

T. Drugan, Ioana Nașcu, P. Grigorescu-Sido, 2017, Scandinavian journal of clinical and laboratory investigation.

Gaucher disease in Romanian patients: incidence of the most common mutations and phenotypic manifestations

C. Caillaud, L. Poenaru, L. Procopciuc, 2002, European Journal of Human Genetics.

Evaluation of neopterin as a biomarker for the monitoring of Gaucher disease patients

N. Miron, T. Drugan, Ioana Nașcu, 2016, Hematology.

GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss

R. Popp, P. Grigorescu-Sido, C. Al-Khzouz, 2017 .

Mucopolysaccharidosis type I - Clinical and genetic characteristics of Romanian patients

C. Lazea, T. Pop, C. Asavoaie, 2020 .

Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type II.

É. Kiss, C. Lazea, Ioana Nașcu, 2016, JIMD reports.

Dynamic changes of lipid profile in Romanian patients with Gaucher disease type 1 under enzyme replacement therapy: a prospective study

D. Leucuta, K. Lackner, H. Rossmann, 2013, Journal of Inherited Metabolic Disease.

Baseline characteristics and outcome in Romanian patients with Gaucher disease type 1.

C. Coldéa, A. Zimmermann, M. Grigorescu, 2010, European journal of internal medicine.

Results of interferon treatment in children with chronic hepatitis B.

V. Creț, P. Grigorescu-Sido, Anca Grigorescu-Sido, 2002, Romanian journal of gastroenterology.

16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the Literature

C. Lazea, C. Asavoaie, P. Grigorescu-Sido, 2020, Frontiers in Pediatrics.

Mutational Analysis and Genotype-Phenotype Correlation in Patients with Classic 21-Hydroxylase Deficiency from Transylvania (North-West Romania)

U. Heinrich, E. Schulze, P. Grigorescu-Sido, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Molecular and Cytogenetic Analysis of Romanian Patients with Differences in Sex Development

I. Pascanu, L. Blaga, G. Zaharie, 2021, Diagnostics.

Problems in the Diagnosis of Cyclic Vomiting Syndrome in Children.

L. Trandafir, A. Tudose, P. Grigorescu-Sido, 2016, Maedica.

Three New 46,XX Male Patients: A Clinical, Cytogenetic and Molecular Analysis

A. Jauch, P. Vogt, M. Bettendorf, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiency

S. Amselem, M. Legendre, C. Lazea, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIa

H. Rossmann, A. Zimmermann, P. Grigorescu-Sido, 2016, Case reports in genetics.

Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1

D. Leucuta, H. Rossmann, A. Zimmermann, 2018, Therapeutics and clinical risk management.

Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania.

A. Trifa, R. Popp, P. Grigorescu-Sido, 2010, International journal of pediatric otorhinolaryngology.

Diagnostic, treatment and outcome possibilities in achondroplasia

C. Asavoaie, P. Grigorescu-Sido, Simona Bucerzan, 2021, Medicine and pharmacy reports.

Cardiovascular manifestations in Marfan syndrome

G. Cismaru, C. Lazea, P. Grigorescu-Sido, 2021, Medicine and pharmacy reports.

Evaluation of c677t and a1298c polymorphism of the methylenetetrahydrofolate reductase gene as a maternal risk factor for trisomy 21 (a monocentric study)

R. Nicolaescu, C. Lazea, R. Popp, 2017 .